United States · FDA National Drug Code directory
Diethylpropion Hydrochloride ER
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 71335-0049_c150ef3f-41d3-445b-b566-4d672759a1d7
- Product NDC
- 71335-0049
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- Diethylpropion Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20111024
- Source listing expiry
- 20261231
Source-listed ingredients
- DIETHYLPROPION HYDROCHLORIDE — 75 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0049-1) · 71335-0049-1
- 28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0049-2) · 71335-0049-2
- 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0049-3) · 71335-0049-3
- 7 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0049-4) · 71335-0049-4
- 14 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0049-5) · 71335-0049-5
- 84 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0049-6) · 71335-0049-6
- 21 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0049-7) · 71335-0049-7
- 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0049-8) · 71335-0049-8
- 45 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0049-9) · 71335-0049-9
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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